Indole-3-butyric acid synthesis in ecotypes and mutants of Arabidopsis thaliana under different growth conditions

Journal of Plant Physiology

Volumn 164, Issue 1, 2007, Pages 47-59

  Ludwig Müller, Jutta ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

Arabidopsis thaliana; Drought stress; Hormone mutants; Indole 3 butyric acid; Light

Indexed keywords

BIOSYNTHESIS; GENES; MUTAGENESIS; ORGANIC ACIDS;

ARABIDOPSIS THALIANA; DROUGHT STRESS; HORMONE MUTANTS; INDOLE-3-BUTYRIC ACID;

CROPS;

BIOSYNTHESIS; FARM CROPS; GENES; MUTAGENS; ORGANIC ACIDS;

ARABIDOPSIS; ARABIDOPSIS THALIANA; ZEA MAYS;

EID: 33845876874     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2005.10.008     Document Type: Article

References (64)

1. Bartel B., and Fink G. ILR1, an amidohydrolase that releases active indole-3-acetic acid from conjugates. Science 268 (1995) 1745-1748
2. Bartel B., LeClere S., Magidin M., and Zolman B.K. Inputs to the active indole-3-acetic acid pool: de novo synthesis, conjugate hydrolysis, and indole-3-butyric acid ß-oxidation. J Plant Growth Regul 20 (2001) 198-216
3. Benfey P.N., Linstead P.J., Roberts K., Schiefelbein J.W., Hauser M.T., and Aeschbacher R.A. Root development in Arabidopsis: four mutants with dramatically altered root morphogenesis. Development 119 (1993) 57-70
4. Bennett M.J., Marchant A., and Green H.G. Arabidopsis AUX1 gene: a permease-like regulator of root gravitropism. Science 273 (1996) 948-950
5. Boerjan W., Cervera M.T., Delarue M., Beeckman T., Dewitte W., Bellini C., et al. Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction. Plant Cell 7 (1995) 1405-1420
6. Cabrera Y., Poch H.L., Peto C.A., and Chory J. A mutation in the Arabidopsis DET3 gene uncouples photoregulated leaf development from gene expression and chloroplast biogenesis. Plant J 4 (1993) 671-682
7. Campanella J.J., Olajide A., Magnus V., and Ludwig-Müller J. A novel auxin conjugate hydrolase from Triticum aestivum with substrate specificity for longer side-chain auxin amide conjugates. Plant Physiol 135 (2004) 2230-2240
8. Chae H.S., Faure F., and Kieber J.J. The eto1, eto2, and eto3 mutations and cytokinin treatment increase ethylene biosynthesis in Arabidopsis by increasing the stability of ACS protein. Plant Cell 15 (2003) 545-559
9. Chen K.-H., Miller A.N., Patterson G.W., and Cohen J.D. A rapid and simple procedure for purification of indole-3-acetic acid prior to GC-SIM-MS analysis. Plant Physiol 86 (1988) 82-825
10. Chhun T., Taketa S., Tsurumi S., and Ichii M. The effects of auxin on lateral root initiation and root gravitropism in a lateral rootless mutant Lrt1 of rice (Oryza sativa L.). Plant Growth Regul 39 (2003) 161-170
11. Chory J., and Peto C.A. Mutations in the DET1 gene affect cell-type-specific expression of light-regulated genes and chloroplast development in Arabidopsis. Proc Natl Acad Sci USA 87 (1990) 8776-8780
12. Chory J., Nagpal P., and Peto C.A. Phenotypic and genetic analysis of det2, a new mutant that affects light-regulated seedling development in Arabidopsis. Plant Cell 3 (1991) 445-460
13. Cohen J.D. Convenient apparatus for the generation of small amounts of diazomethane. J Chromatogr 303 (1984) 193-196
14. In: Davies P.J. (Ed). Plant hormones. Physiology, biochemistry and molecular biology (1995), Kluwer Academic Publishers, Dordrecht, The Netherlands
15. Delarue M., Muller P., Bellini C., and Delbarre A. Increased auxin efflux in the IAA-overproducing sur1 mutant of Arabidopsis thaliana: a mechanism of reducing auxin levels?. Physiol Plant 107 (1999) 120-127
16. Epstein E., and Lavee S. Conversion of indole-3-butyric acid to indole-3-acetic acid by cuttings of grapevine (Vitis vinifera) and olive (Olea europea). Plant Cell Physiol 25 (1984) 697-703
17. Epstein E., and Ludwig-Müller J. Indole-3-butyric acid in plants: occurrence, biosynthesis, metabolism, and transport. Physiol Plant 88 (1993) 382-438
18. Gamborg O.L.R., Miller R.A., and Ojima K. Nutrient requirements of suspension cultures of soybean root cells. Exp Cell Res 50 (1968) 151-158
19. Guzman P., and Ecker J.R. Exploiting the triple response of Arabidopsis to identify ethylene-related mutants. Plant Cell 2 (1990) 513-523
20. Hauser M.-T., Morikami A., and Benfey P.N. Conditional root expansion mutants of Arabidopsis. Development 121 (1995) 1237-1252
21. Ilić N., Normanly J., and Cohen J.D. Quantification of free plus conjugated indoleacetic acid in Arabidopsis requires correction for nonenzymatic conversion of indolic nitriles. Plant Physiol 111 (1996) 781-788
22. Jackson R.G., Kowalczyk M., Li Y., Higgins G., Ross J., Sandberg G., et al. Over-expression of an Arabidopsis gene encoding a glucosyltransferase of indole-3-acetic acid: phenotypic characterisation of transgenic lines. Plant J 32 (2002) 573-583
23. Kaldorf M., and Ludwig-Müller J. AM fungi might affect the root morphology of maize by increasing indole-3-butyric acid biosynthesis. Physiol Plant 109 (2000) 58-67
24. Kreps J.A., Ponappa T., Dong W., and Town C.D. Molecular basis of α-methyltryptophan resistance in amt-1, a mutant of Arabidopsis thaliana with altered tryptophan metabolism. Plant Physiol 110 (1996) 1159-1165
25. LeClere S., Tellez R., Rampey R.A., Matsuda S.P.T., and Bartel B. Characterization of a family of IAA-amino acid conjugate hydrolases from Arabidopsis. J Biol Chem 277 (2002) 20446-20452
26. Lehman A., Black R., and Ecker J.R. HOOKLESS1, an ethylene response gene, is required for differential cell elongation in the Arabidopsis hypocotyl. Cell 85 (1996) 183-194
27. Lemieux B., Miquel M., Somerville C., and Browse J. Mutants of Arabidopsis with alterations in seed lipid fatty acid composition. Theor Appl Genet 80 (1990) 234-240
28. Li H.M., Altschmied L., and Chory J. Arabidopsis mutants define downstream branches in the phototransduction pathway. Genes Dev 8 (1994) 339-349
29. Li J., Nagpal P., Vitart V., McMorris T.C., and Chory J. A role for brassinosteroids in light-dependet development of Arabidopsis. Science 272 (1996) 398-401
30. Ludwig-Müller J. The biosynthesis of auxins. Curr Topics Plant Biol 1 (1999) 77-88
31. Ludwig-Müller J. Indole-3-butyric acid in plant growth and development. Plant Growth Regul 32 (2000) 219-230
32. Ludwig-Müller J., and Epstein E. Occurrence and in vivo biosynthesis of indole-3-butyric acid in corn (Zea mays L). Plant Physiol 97 (1991) 765-770
33. Ludwig-Müller J., and Epstein E. Indole-3-butyric acid in Arabidopsis thaliana. II. In vivo metabolism. Plant Growth Regul 13 (1993) 189-195
34. Ludwig-Müller J., and Epstein E. Indole-3-butyric acid in Arabidopsis thaliana. III. In vivo biosynthesis. Plant Growth Regul 14 (1994) 7-14
35. Ludwig-Müller J., and Hilgenberg W. Characterization and partial purification of indole-3-butyric acid synthetase from maize (Zea mays). Physiol Plant 94 (1995) 651-660
36. Ludwig-Müller J., and Cohen J.D. Identification and quantification of three active auxins in different tissues of Tropaeolum majus. Physiol Plant 115 (2002) 320-329
37. Ludwig-Müller J., Sass S., Sutter E.G., Wodner M., and Epstein E. Indole-3-butyric acid in Arabidopsis thaliana. I. Identification and quantification. Plant Growth Regul 13 (1993) 179-187
38. Ludwig-Müller J., Hilgenberg W., and Epstein E. The in vitro biosynthesis of indole-3-butyric acid in maize. Phytochemistry 40 (1995) 61-68
39. Ludwig-Müller J., Schubert B., and Pieper K. Regulation of IBA synthetase by drought stress and abscisic acid. J Exp Bot 46 (1995) 423-432
40. Ludwig-Müller J., Kaldorf M., Sutter E.G., and Epstein E. Indole-3-butyric acid (IBA) is enhanced in young maize (Zea mays L.) roots colonized with the arbuscular mycorrhizal fungus Glomus intraradices. Plant Sci 125 (1997) 153-162
41. Ludwig-Müller J., Schubert B., Rademacher W., and Hilgenberg W. Indole-3-butyric acid biosynthesis in maize is enhanced by cyclohexanedione herbicides. Physiol Plant 110 (2000) 544-550
42. Ludwig-Müller J., Vertocnik A., and Town C.D. Analysis of indole-3-butyric acid induced adventitious root formation on Arabidopsis stem segments. J Exp Bot 56 (2005) 2095-2105
43. Ludwig-Müller J., Walz A., Slovin J.P., Epstein E., Cohen J.D., Dong W., et al. Overexpression of the iaglu gene from maize in Arabidopsis thaliana alters plant growth and sensitivity to IAA but not IBA and 2,4-D. J Plant Growth Regul 24 (2005) 127-141
44. Mikkelsen M.D., Naur P., and Halkier B.A. Arabidopsis mutants in the C-S lyase of glucosinolate biosynthesis establish a critical role for indole-3-acetaldoxime in auxin homeostasis. Plant J 37 (2004) 770-777
45. Murashige T., and Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15 (1962) 473-497
46. Nordström A.-C., Jacobs F.A., and Eliasson L. Effect of exogenous indole-3-acetic acid and indole-3-butyric acid on internal levels of the respective auxins and their conjugation with aspartic acid during adventitious root formation in pea cuttings. Plant Physiol 96 (1991) 856-861
47. Normanly J., Grisafi P., Fink G.R., and Bartel B. Arabidopsis mutants resistant to the auxin effects of indole-3-acetonitrile are defective in the nitrilase encoded by the NIT1 gene. Plant Cell 9 (1997) 1781-1790
48. Pickett F.B., Wilson A.K., and Estelle M. The axr1 mutation of Arabidopsis confers both auxin and ethylene resistance. Plant Physiol 94 (1990) 1462-1466
49. Poupart J., and Waddell C. The rib1 mutant is resistant to indole-3-butyric acid, an endogenous auxin in Arabidopsis. Plant Physiol 124 (2000) 1739-1751
50. Rashotte A.M., Poupart J., Waddell C.S., and Muday G.K. Transport of the two natural auxins, indole-3-butyric acid and indole-3-acetic acid, in Arabidopsis. Plant Physiol 133 (2003) 761-772
51. Rock C.D., and Zeevaart J.A.D. The aba mutant of Arabidopsis thaliana is impaired in epoxy-carotenoid biosynthesis. Proc Natl Acad Sci USA 88 (1991) 7496-7499
52. Rose A.B., Li J., and Last R.L. An allelic series of blue fluorescent trp1 mutants of Arabidopsis thaliana. Genetics 145 (1997) 197-205
53. Schindelman G., Morikami A., Jung J., Baskin T.I., Carpita N.C., Derbyshire P., et al. COBRA encodes a putative GPI-anchored protein, which is polarly localized and necessary for oriented cell expansion in Arabidopsis. Genes Dev 115 (2001) 1115-1127
54. Schumacher K., Vafeados D., McCarthy M., Sze H., Wilkins T., and Chory J. The Arabidopsis det3 mutant reveals a central role for the vacuolar H(+)-ATPase in plant growth and development. Genes Dev 13 (1999) 3259-3270
55. Schwartz S.H., Léon-Kloosterziel K.M., Koornneef M., and Zeevaart J.A.D. Biochemical characterization of the aba2 and aba3 mutants in Arabidopsis thaliana. Plant Physiol 114 (1997) 161-166
56. Seo M., Akaba S., Oritani T., Delarue M., Bellini C., Caboche M., et al. Higher activity of an aldehyde oxidase in the auxin-overproducing superroot1 mutant of Arabidopsis thaliana. Plant Physiol 116 (1998) 687-693
57. Staswick P.E., Su W.P., and Howell S.H. Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant. Proc Natl Acad Sci USA 89 (1992) 6837-6840
58. Staswick P.E., and Tiryaki I. The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell 16 (2004) 2117-2127
59. Sutter E.G., and Cohen J.D. Measurement of indolebutyric acid in plant tissues by isotope dilution gas chromatography-mass spectrometry analysis. Plant Physiol 99 (1992) 1719-1722
60. Vartanian N., Marcotte L., and Giraudat J. Drought rhizogenesis in Arabidopsis thaliana. Plant Physiol 104 (1994) 761-767
61. Vogel J.P., Woeste K.E., Theologis A., and Kieber J.J. Recessive and dominant mutations in the ethylene biosynthetic gene ACS5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively. Proc Natl Acad Sci USA 95 (1998) 4766-4771
62. Wysocka-Diller J.W., Helariutta Y., Fukaki H., Malamy J.E., and Benfey P.N. Molecular analysis of SCARECROW function reveals a radial patterning mechanism common to root and shoot. Development 127 (2000) 595-603
63. Xiong L., Ishitani M., Lee H., and Zhu J.K. The Arabidopsis LOS5/ABA3 locus encodes a molybdenum cofactor sulfurase and modulates cold stress- and osmotic stress-responsive gene expression. Plant Cell 13 (2001) 2063-2083
64. Zolman B., Yoder A., and Bartel B. Genetic analysis of indole-3-butyric acid response in Arabidopsis thaliana reveals four mutant classes. Genetics 156 (2000) 1323-1327